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大环内酯类药物治疗成人哮喘的疗效与安全性:一项系统评价和荟萃分析。

Efficacy and safety of macrolide therapy for adult asthma: A systematic review and meta-analysis.

作者信息

Fukuda Yosuke, Horita Nobuyuki, Aga Masaharu, Kashizaki Fumihiro, Hara Yu, Obase Yasushi, Niimi Akio, Kaneko Takeshi, Mukae Hiroshi, Sagara Hironori

机构信息

Department of Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, Tokyo, Japan; Department of Medicine, Division of Respiratory Medicine, Yamanashi Red Cross Hospital, Yamanashi, Japan.

Chemotherapy Center, Yokohama City University Hospital, Kanagawa, Japan.

出版信息

Respir Investig. 2024 Mar;62(2):206-215. doi: 10.1016/j.resinv.2023.12.015. Epub 2024 Jan 10.

Abstract

BACKGROUND

The evidence for macrolide therapy in adult asthma is not properly established and remains controversial. We conducted a systematic review and meta-analysis to examine the efficacy and safety of macrolide therapy for adult asthma.

METHODS

We searched randomized controlled trials from MEDLINE via the PubMed, CENTRAL, and Ichushi Web databases. The primary outcome was asthma exacerbation. The secondary outcomes were serious adverse events (including mortality), asthma-related quality of life (symptom scales, Asthma Control Questionnaire, and Asthma Quality of Life Questionnaire), rescue medication (puffs/day), respiratory function (morning peak expiratory flow, evening peak flow, and forced expiratory volume in 1 s), bronchial hyperresponsiveness, and minimum oral corticosteroid dose. Of the 805 studies, we selected seven studies for the meta-analysis, which was conducted using a random-effects model.

SYSTEMATIC REVIEW REGISTRATION

University Hospital Medical Information Network Clinical Trials Registry (UMIN000050824).

RESULTS

No significant difference between macrolide and placebo for asthma exacerbations was observed (risk ratio 0.71, 95 % confidence interval [CI] 0.46-1.09; p = 0.12). Macrolide therapy for adult asthma showed a significant improvement in rescue medication with short-acting beta-agonists (mean difference -0.41, 95 % CI -0.78 to -0.04; p = 0.03). Macrolide therapy did not show more serious adverse events (odd ratio 0.61, 95 % CI 0.34-1.10; p = 0.10) than those with placebo. The other secondary outcomes were not significantly different between the macrolide and placebo groups.

CONCLUSIONS

Macrolide therapy for adult asthma may be more effective than placebo and could be a treatment option.

摘要

背景

大环内酯类药物治疗成人哮喘的证据尚不充分,仍存在争议。我们进行了一项系统评价和荟萃分析,以研究大环内酯类药物治疗成人哮喘的疗效和安全性。

方法

我们通过PubMed、CENTRAL和Ichushi Web数据库检索MEDLINE中的随机对照试验。主要结局是哮喘急性发作。次要结局包括严重不良事件(包括死亡率)、哮喘相关生活质量(症状量表、哮喘控制问卷和哮喘生活质量问卷)、急救药物使用量(每日喷数)、呼吸功能(早晨呼气峰值流速、晚上峰值流速和1秒用力呼气量)、支气管高反应性以及口服糖皮质激素的最小剂量。在805项研究中,我们选择了7项研究进行荟萃分析,采用随机效应模型。

系统评价注册

大学医院医学信息网络临床试验注册库(UMIN000050824)。

结果

在哮喘急性发作方面,未观察到大环内酯类药物与安慰剂之间存在显著差异(风险比0.71,95%置信区间[CI]0.46 - 1.09;p = 0.12)。大环内酯类药物治疗成人哮喘在使用短效β受体激动剂作为急救药物方面有显著改善(平均差 -0.41,95% CI -0.78至 -0.04;p = 0.03)。大环内酯类药物治疗组的严重不良事件(比值比0.61,95% CI 0.34 - 1.10;p = 0.10)并不比安慰剂组更多。大环内酯类药物组和安慰剂组在其他次要结局方面无显著差异。

结论

大环内酯类药物治疗成人哮喘可能比安慰剂更有效,可作为一种治疗选择。

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